GE Medical Systems (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688
www.gehealthcare.com
Revision history
Revision History
Date
Revision
Rev.12014/01/09Initial Release
Rev.22014/03/11Update for transportation box
Rev.32016/06/30Update spare part list
Rev.42016/11/18Update spare part list
Rev.52017/08/23Update spare part list
PagesRevisionPagesRevision
FrontRev. 5Chapter 6Rev. 5
Front matterRev. 5Chapter 7Rev. 5
TOCRev. 5Chapter 8Rev. 5
(YYYY/MM/DD)Reason for change
List of Effected Pages (LOEP)
Chapter 1Rev. 5Chapter 9Rev. 5
Chapter 2Rev. 5Chapter 10Rev. 5
Chapter 3Rev. 5IndexRev. 5
Chapter 4Rev. 5Rear CoverRev. 5
Chapter 5Rev. 5
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product
Data Management). If you need to know the latest revision, contact your distributor, local
GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at
1 800 682 5327 or 1 262 524 5698.
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Important precautions
Translation policy
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Damage in transportation
All packages should be closely examined at time of delivery. If
damage is apparent, write “Damage In Shipment” on ALL copies
of the freight or express bill BEFORE delivery is accepted or
“signed for” by a GE representative or hospital receiving agent.
Whether noted or concealed, damage MUST be reported to the
carrier immediately upon discovery, or in any event, within 14
days after receipt, and the contents and containers held for
inspection by the carrier. A transportation company will not pay a
claim for damage if an inspection is not requested within this 14
day period.
Certified electrical contractor statement - For USA Only
All electrical Installations that are preliminary to positioning of
the equipment at the site prepared for the equipment shall be
performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing
shall be performed by qualified GE personnel. In performing all
electrical work on these products, GE will use its own specially
trained field engineers. All of GE’s electrical work on these
products will comply with the requirements of the applicable
electrical codes.
The purchaser of GE equipment shall only utilize qualified
personnel (i.e., GE’s field engineers, personnel of third-party
service companies with equivalent training, or licensed
electricians) to perform electrical servicing on the equipment.
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Omission and errors
If there are any omissions, errors or suggestions for improving
this documentation, contact the GE Global Documentation
Group with specific information listing the system type, manual
title, part number, revision number, page number and
suggestion details.
Mail the
information to:
GE Medical Systems (China) Co., Ltd.
No. 19 Changiang Road
Wuxi National Hi-Tech Dev. Zone
Jiangsu
P.R.China 214028
GE employees should use TrackWise to report service
documentation issues.
These issues will then be in the internal problem reporting tool
and communicated to the writer.
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Service Safety Considerations
WARNING
DANGERDANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,
ARE PRESENT IN THIS EQUIPMENT. USE EXTREME
CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
Use all Personal Protection Equipment (PPE) such as gloves,
safety shoes, safety glasses, and kneeling pad, to reduce the
risk of injury.
For a complete review of all safety requirements, refer to
Chapter 1 in the Service Manual.
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Legal notes
Trademarks
Copyrights
The contents of this publication may not be copied or duplicated
in any form, in whole or in part, without prior written permission
of GE.
GE may revise this publication from time to time without written
notice.
All products and their name brands are trademarks of their
respective holders.
This chapter describes important issues related to
safely servicing the Ultrasound system. The service
provider must read and understand all the information
presented here before installing or servicing the units.
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Introduction
Contents in this chapter
• ‘Overview’ on page 1-2
• ‘Manual Overview’ on page 1-3
• ‘Important conventions’ on page 1-6
• ‘Product icons’ on page 1-10
• ‘Labels locations’ on page 1-11
• ‘Safety considerations’ on page 1-12
• ‘Dangerous procedure warnings’ on page 1-20
• ‘Lockout/Tagout (LOTO) requirements’ on page 1-21
• ‘Returning probes and repair parts’ on page 1-22
• ‘EMC, EMI and ESD’ on page 1-23
• ‘Customer assistance’ on page 1-25
Overview
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This manual provides installation and service information for the
LOGIQ C9 Series Ultrasound system. It is divided in ten
chapters as shown below.
Contents in this manual
The manual is divided into ten chapters.
In the beginning of the manual, before chapter 1, you will find
the Revision overview, the Important precautions including
Translation policy, Damage in transportation, Certified electrical
contractor statement, Omission & errors, Service safety
considerations and Legal notes, and the Table of Contents
(TOC).
Manual Overview
Manual Overview
Chapter
number
1.
2.
3.
4.
5.
6.
An Index has been included after Chapter 10.
Table 1-1: Contents in this manual
Chapter titleDescription
IntroductionContains a content summary and warnings.
Site preparationsContains pre-setup requirements for the LOGIQ
C9 Series.
System SetupContains setup procedure with procedure
checklist for the system.
General Procedures
and Functional
Checks
Components and
Functions (Theory)
Service AdjustmentsContains instructions on how to make any
Contains functional checks that must be
performed as part of the installation, or as
required during servicing and periodic
maintenance.
Contains block diagrams and functional
explanations of the electronics.
available adjustments to the LOGIQ C9 Series.
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Introduction
Table 1-1: Contents in this manual (Continued)
Chapter
Chapter titleDescription
number
7.
8.
9.
Diagnostics/
Troubleshooting
Replacement
procedures
Provides procedures for running diagnostic or
related routines for the LOGIQ C9 Series.
Provides disassembly procedures and
reassembly procedures for all changeable FRU.
Renewal PartsContains a complete list of replacement parts for
LOGIQ C9 Series.
10.
Care & MaintenanceProvides periodic maintenance procedures for
LOGIQ C9 Series.
N/AIndexA quick way to the topic you’re looking for.
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LOGIQ C9 Series models covered by this manual
Table 1-2: LOGIQ C9 Series Model Designations
Model NumberDescriptionSystem SW
5489329LOGIQ C9 Premium for ChinaR1.x.x
5489330LOGIQ C9 Expert for China (with 4D)R1.x.x
5489331LOGIQ C9 Expert for ChinaR1.x.x
5489332LOGIQ C9 Expert for IndiaR1.x.x
NOTE: When not otherwise specified, the contents of this manual
applies to all LOGIQ C9 Series models.
Manual Overview
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Introduction
Conventions used in book
Important conventions, used in this document, are described
next.
Model designations
This manual covers the LOGIQ C9 Series Ultrasound systems
listed in:
‘LOGIQ C9 Series models covered by this manual’ on page 1-5.
Icons
Important conventions
Pictures, or icons, are used wherever they will reinforce the
printed message. The icons, labels, and conventions used on
the product and in the service information are described in this
chapter.
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Safety precaution messages
DANGER
WARNING
CAUTION
Various levels of safety precaution messages may be found on
the equipment and in the service information. The different
levels of concern are identified by a flag word that precedes the
precautionary message. Known or potential hazards to
personnel are labeled in one of three ways:
• DANGER
• WARNING
• CAUTION
Danger is used to indicate the presence of a hazard that will
cause severe personal injury or death if the instructions are
ignored.
Warning is used to indicate the presence of a hazard that can
cause severe personal injury and property damage if
instructions are ignored.
Important conventions
Caution is used to indicate the presence of a hazard that will or
can cause minor personal injury and property damage if
instructions are ignored. Equipment damage possible.
NOTE: Notes are used to provide important information about an item
or a procedure.
NOTE: Be sure to read the notes; the information contained in a note
can often save you time or effort.
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Introduction
Standard hazard icons
Important information will always be preceded by either the
exclamation point (!) contained within a triangle, or the symbols
for “Danger”, “Warning” or “Caution”, as seen throughout this
chapter. In addition to text, several different graphical icons
(symbols) may be used to make you aware of specific types of
hazards that could possibly cause harm. Even if a symbol isn’t
used in this manual, it may be included for your reference.
Table 1-3: Standard hazard icons
ELECTRICAL
MECHANICAL
RADIATION
LASER
HEAT
PINCH
NOTE: Even if a symbol isn’t used on the product or in this manual, it
may be included for your reference.
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Important conventions
Standard Icons that indicate that a special procedure is to be used
Some others icons make you aware of specific procedures that
should be followed.
Table 1-4: Standard Icons that indicates that a special procedure is to be used
Avoid Static ElectricityTag and Lock OutWear Eye Protection
Hand ProtectionFoot ProtectionWear Eye Protection
Be sure to read the notes; the information contained in a note
can often save you time or effort.
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Introduction
Product icons
It is important to refer to the current revision of the Ultrasound
system’s User Manual for a full list of product labels prior to
servicing the system.
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Labels locations
Labels locations
It is important to refer to the current revision of the Ultrasound
system’s User Manual for a full list of product labels prior to
servicing the system.
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Introduction
DANGER
WARNING
Contents in this section
• ‘Introduction’ on page 1-12
• ‘Human Safety’ on page 1-12
• ‘Mechanical safety’ on page 1-15
• ‘Electrical safety’ on page 1-18
Introduction
The following safety precautions must be observed during all
phases of operation, service and repair of this equipment.
Failure to comply with these precautions or with specific
warnings elsewhere in this manual, violates safety standards of
design, manufacture and intended use of the equipment.
Safety considerations
Human Safety
• Operating personnel must not remove the system covers.
• Servicing should be performed by authorized personnel
only.
Only personnel who have participated in a LOGIQ C9 Series
Training Seminar are authorized to service the equipment.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING
DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
If the covers are removed from an operating LOGIQ C9 Series,
some metal surfaces may be warm enough to pose a potential
heat hazard if touched, even while in shutdown mode.
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Human Safety (continued)
WARNING
WARNING
WARNING
WARNING
WARNING
Because of the limited access to cabinets and equipment in the
field, placing people in awkward positions, GE has limited the
lifting weight for one person in the field to 16 KG (35 LBS).
Anything over 16 KG (35 LBS) requires 2 people.
Have two people available to deliver and unpack the LOGIQ
C9 Series.
Attempts to move the Ultrasound system considerable
distances or on an incline by one person could result in injury
or damage or both.
Explosion Warning
DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.
Safety considerations
DO NOT substitute parts or modify equipment
Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.
Ensure that the Ultrasound system is turned off and unplugged
Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light on
the OP panel ON/OFF button will turn off.
Ultrasound system components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions
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Introduction
WARNING
WARNING
WARNING
WARNING
Human Safety (continued)
Risk of electrical shock, Ultrasound system must be turned off
and disconnected from power source. Cord must be controlled
at all times.
Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light on
the OP panel on/off button will turn off.
Ultrasound System components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions
Use all Personal Protection Equipment (PPE) such as gloves,
safety shoes, safety glasses, and kneeling pad, to reduce the
risk of injury.
Beware of possible sharp edges on all mechanical parts. If
sharp edges are encountered, the appropriate PPE should be
used to reduce the risk of injury.
Wear all PPE including gloves as indicated in the chemical
MSDS.
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Mechanical safety
WARNING
WARNING
WARNING
WARNING
CAUTION
CAUTION
Safety considerations
While the software install procedure is designed to preserve
data, you should save any patient data, images, system setups
to removable media or hardcopy before doing a software
upgrade.
Ultrasound probes are highly sensitive medical instruments
that can easily be damaged by improper handling. Use care
when handling and protect from damage when not in use. Do NOT use a damaged or defective probe. Failure to follow these
precautions can result in serious injury and equipment
damage.
Never use a probe that has fallen to the floor. Even if it looks
OK, it may be damaged.
When the Ultrasound system is raised for a repair or moved
along any incline, use extreme caution since it may become
unstable and tip over.
Take extra care when moving the system.
The LOGIQ C9 Series weighs approximately 130 kg (287 lbs)
or more, depending on installed peripherals, when ready for
use. To avoid possible injury and equipment damage when
transporting from one area of use to another:
• Be sure the pathway is clear.
• Limit movement to a slow careful walk.
• Use two or more persons to move the equipment on
inclines or long distance.
Before you move or transport the Ultrasound system, make
sure to lock the LCD monitor arm firmly and flip down the
monitor to prevent damage to the Ultrasound system.
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Introduction
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
Mechanical safety (continued)
To avoid injury when you move the LCD monitor and the
monitor arm, do not put your finger, hand, or object on the joint
of the monitor or the monitor arm.
Ensure that nobody touches the console arm when moving the
operator panel.
Do not move the Ultrasound system if the Operator Panel is in
unlocked position.
Do not transport LOGIQ C9 Series in a vehicle without locking
the casters (wheels) and securing it as described in chapter 4.
Use protective glasses during drilling, filing smooth surfaces,
and during all other work where eyes need protection.
Use safety shoes when doing work where there is any chance
of foot injury.
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Mechanical safety (continued)
CAUTION
CAUTION
Use protective gloves when working with sharp edges or when
directed to wear PPE during a removal/replacement procedure.
Be careful not to pinch any of the cables.
NOTE: Special care should be taken when transporting the Ultrasound
system in a vehicle:
• Before transporting, place the system in its special storage
case.
• Lock the wheels (brake)
• Ensure that the system is firmly secured while inside the
vehicle.
• Secure system with straps or as directed otherwise to
prevent motion during transport.
• Prevent vibration damage by driving cautiously. Avoid
unpaved roads, excessive speeds, and erratic stops or
starts.
Safety considerations
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Introduction
WARNING
Electrical safety
Safe practices
Follow these guidelines to minimize shock hazards whenever
you are using the Ultrasound system:
• To minimize shock hazard, the equipment chassis must be
connected to an electrical ground.
• The Ultrasound system is equipped with a three-conductor
AC power cable. This must be plugged into an approved
electrical outlet with safety ground.
• The power outlet used for this equipment should not be
shared with other types of equipment.
• Both the system power cable and the power connector must
meet international electrical standards
Connecting a LOGIQ C9 Series to the wrong voltage level will
most likely destroy it.
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Probes
Safety considerations
Follow these guidelines before connecting a probe to the
Ultrasound system:
• Inspect the probe prior to each use for damage or
degradation to the:
• housing
• cable strain relief
• lens
• seal
• connector pins
• locking mechanism
• Do not use a damaged or defective probe.
• Never immerse the probe connector or adapter into any
liquid.
• The system has more than one type of probe port. Use the
appropriate probe port designed for the probe you are
connecting.
Peripherals
Refer to the Patient Safety Environment section of the User’s
Manual for peripheral isolation information.
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Introduction
DANGER
WARNING
WARNING
WARNING
WARNING
Dangerous procedure warnings
Warnings, such as the example below, precede potentially
dangerous procedures throughout this manual. Instructions
contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING
DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
If the covers are removed from an operating LOGIQ C9 Series,
some metal surfaces may be warm enough to pose a potential
heat hazard if touched, even while in shutdown mode.
Explosion Warning
DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.
DO NOT substitute parts or modify equipment
Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC
INVALID MAY CAUSE THE DAMAGE OF SYSTEM
FILES.
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Lockout/Tagout (LOTO) requirements
WARNING
Lockout/Tagout (LOTO)
requirements
Follow Lockout/Tagout requirements by ensuring you are in total
control of the AC power plug at all times during the service
process.
To apply Lockout/Tagout (LOTO):
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Remove/disconnect the battery, if present.
5. Apply Lockout/Tagout Devices.
6. Control all stored and residual energy.
7. Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Energy Control and Power Lockout for LOGIQ C9 Series.
When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.
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Introduction
Returning probes and repair parts
Equipment being returned must be clean and free of blood and
other infectious substances. GE policy states that body fluids
must be properly removed from any part or equipment prior to
shipment. GE employees, as well as customers, are responsible
for ensuring that parts/equipment have been properly
decontaminated prior to shipment. Under no circumstance
should a part or equipment with visible body fluids be taken or
shipped from a clinic or site (for example, body coils or an
ultrasound probe).
The purpose of the regulation is to protect employees in the
transportation industry, as well as the people who will receive or
open this package.
NOTE: The US Department of Transportation (DOT) has ruled that
“items that were saturated and/or dripping with human blood
that are now caked with dried blood; or which were used or
intended for use in patient care” are “regulated medical waste”
for transportation purposes and must be transported as a
hazardous material.
NOTE: The USER/SERVICE staff should dispose of all the waste
properly, per federal, state, and local waste disposal regulations.
The Ultrasound system is not meant to be used for long-term
storage of patient data or images. The user is responsible for the
data on the system and a regular backup is highly
recommended.
If the system is sent for repair, please ensure that any patient
information is backed up and erased from the system before
shipping. It is always possible during system failure and repair to
lose patient data. GE is not responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to
GE employees for service purposes, GE will ascertain
agreement from the customer. Patient information shall only be
transferred by approved service processes, tools and devices
restricting access, protecting or encrypting data where required,
and providing traceability in the form of paper or electronic
documents at each stage of the procedure while maintaining
compliance with cross-border restrictions of patient information
transfers.
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What is EMC?
EMC, EMI and ESD
EMC, EMI and ESD
Electromagnetic compatibility describes a level of performance
of a device within its electromagnetic environment. This
environment consists of the device itself and its surroundings
including other equipment, power sources and persons with
which the device must interface. Inadequate compatibility results
when a susceptible device fails to perform as intended due
interference from its environment or when the device produces
unacceptable levels of emission to its environment. This
interference is often referred to as radio–frequency or
electromagnetic interference (RFI/EMI) and can be radiated
through space or conducted over interconnecting power of
signal cables. In addition to electromagnetic energy, EMC also
includes possible effects from electrical fields, magnetic fields,
electrostatic discharge and disturbances in the electrical power
supply.
CE Compliance
LOGIQ C9 Series conforms to all applicable conducted and
radiated emission limits and to immunity from electrostatic
discharge, radiated and conducted RF fields, magnetic fields
and power line transient requirements.
For applicable standards, refer to the Safety Chapter of the
Ultrasound system’s User’s Manual.
NOTE: For CE Compliance, it is critical that all covers, screws,
shielding, gaskets, mesh, clamps, are in good condition,
installed tightly without skew or stress. Proper installation
following all comments noted in this service manual is required
in order to achieve full EMC performance.
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Introduction
WARNING
WARNING
Electrostatic discharge (ESD) prevention
DO NOT touch any boards with integrated circuits prior to
taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound
system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive
equipment.
Risk of electrical shock, Ultrasound system must be turned off.
Avoid all contact with electrical contacts, conductors and
components. Always use non-conductive handles designed for
the removal and replacement of ESD sensitive parts. All parts
that have the potential for storing energy must be discharged or
isolated before making contact.
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Contact information
Customer assistance
Customer assistance
If this equipment does not work as indicated in this service
manual or in the user manual, or if you require additional
assistance, please contact the local distributor or appropriate
support resource, as listed below.
Before you call, identify the following information, and acquire
image (Alt+D) to send to the Customer Care team:
1. System ID serial number.
2. Software version.
3. Date and time of occurrence.
4. Sequence of events leading to issue.
5. Is the issue repeatable?
6. Imaging mode, probe, preset/application.
7. Media brand, speed, capacity, type.
8. Save secondary image capture, cine loop, 4D multi-volume
loop.
NOTE: Restart the application before resuming clinical scanning.
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Introduction
Phone numbers for Customer Assistance
Table 1-5: Phone numbers for Customer Assistance
LOCATIONPHONE NUMBER
USA
GE Healthcare - GE Medical Systems
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
CanadaPhone:1-800-668-0732
Latin AmericaService
Europe (OLC-EMEA)
GE Ultraschall Deutschland Gmbh & Co. KG
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany
GE Medical Systems (China) Co., Ltd.
No.19 Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu
P.R.China 214028
+86 510 85225888+86 510 85226688
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Authorized Representative
Table 1-7: Authorized Representative
AUTHORIZED REPRESENTATIVE
Customer assistance
TELEPHONE / FAX
NUMBER
The location of the CE marking is shown in the Safety chapter of the User
manual.
Authorized EU Representative/European registered place of business:
GE Medical Systems Information Technologies GmbH (GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY
+49 761 45 43 -0 /
+49 761 45 43 -233
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Introduction
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Chapter 2
Site Preparations
This chapter provides the information required to plan
and prepare for the setup of an Ultrasound system.
Included are descriptions of the facility and electrical
needs to be met by the purchaser of the units.
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Site Preparations
Contents in this chapter
• ‘Overview’ on page 2-2
• ‘General Ultrasound system requirements’ on page 2-3
• ‘Facility needs’ on page 2-12
• ‘Environmental Dangers’ on page 2-22
Overview
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General Ultrasound system
CAUTION
Contents in this section
• ‘Ultrasound system environmental requirements’ on
page 2-3
• ‘Electrical requirements’ on page 2-6
• ‘EMI limitations’ on page 2-9
• ‘Probes environmental requirements’ on page 2-11
• ‘Time and manpower requirements’ on page 2-11
General Ultrasound system requirements
requirements
Ultrasound system environmental requirements
If the Ultrasound system is very cold or hot
When unpacking the Ultrasound system, allow the temperature
of the Ultrasound system to stabilize before powering up. The
following table describes guidelines for reaching operational
temperatures from storage or transport temperatures.
If the Ultrasound system is very cold or hot, do not turn on its
power until it has had a chance to acclimate to its operating
environment.
Table 2-1: System Acclimation Time Chart
Degree C50454035302520151050-5
Degree F122113104958677685950413223
hours4 2 0 000000246
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Site Preparations
CAUTION
CAUTION
Environmental specifications for Ultrasound system
The system should be operated, stored, or transported within
the parameters outlined below. Either its operational
environment must be constantly maintained or the unit must be
turned off.
Table 2-2: System Environmental Requirements
OperationalStorageTransport (<16hrs.)
Temperature10° - 40°C
50° - 104°F
Humidity30 - 80%
non-condensing
Pressure700 - 1060hPa700 - 1060hPa700 - 1060hPa
Ensure that the probe face temperature does not exceed the
normal operation temperature range.
The LOGIQ C9 Series system and probe connector is not
waterproof. Do not expose the device to water or any kind of
liquid.
-5° - 50°C
23° - 122°F
10 - 90%
non-condensing
-5° - 50°C
23° - 122°F
10 - 90%
non-condensing
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Cooling
Lighting
General Ultrasound system requirements
The cooling requirement for a console Ultrasound system with
monitor and on board peripherals, is up to 3800 BTU/h. This
figure does not include cooling needed for lights, people, or
other equipment in the room.
NOTE: Each person in the room places an additional 300 BTU/h
demand on the cooling system.
Bright light is needed for Ultrasound system installation, updates
and repairs. However, operator and patient comfort may be
optimized if the room light is subdued and indirect. Therefore a
combination lighting system (dim/bright) is recommended. Keep
in mind that lighting controls and dimmers can be a source of
EMI which could degrade image quality. These controls should
be selected to minimize possible interference.
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Electrical requirements
General requirements
NOTE: GE requires a dedicated power and ground for the proper
operation of its Ultrasound equipment. This dedicated power
shall originate at the last distribution panel before the Ultrasound
system.
Sites with a mains power system with defined Neutral and Live
The dedicated line shall consist of one phase, a neutral (not
shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral
The dedicated line shall consist of one phase (two lines), not
shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within
the facility, the ground from the main facility's incoming power
source to the Ultrasound system is only a conduit.
Electrical requirements for the Ultrasound system
In the table below, the electrical specifications for the Ultrasound
system includes monitor and on board peripherals.
Table 2-3: Electrical Specifications for LOGIQ C9 Series system
Vol tag e
To le r an c ePower ConsumptionFrequency
:
:
220-240 VAC
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±10%Max. 950VA50/ 60HZ
5482298-100 English Rev. 5
Site circuit breaker
CAUTION
CAUTION
Site power outlets
General Ultrasound system requirements
Power outage may occur. The LOGIQ C9 Series requires a
dedicated single branch circuit. To avoid circuit overload and
possible loss of critical care equipment, make sure you do not
have any other equipment operating on the same circuit.
It is recommended that the branch circuit breaker for the
Ultrasound system be readily accessible.
POWER OUTAGE MAY OCCURE.
The LOGIQ C9 Series requires a dedicated single branch
circuit. To avoid circuit overload and possible loss of critical
care equipment, make sure you DO NOT have any other
equipment operating on the same circuit.
Unit power plug
A dedicated AC power outlet must be within reach of the
Ultrasound system without extension cords. Other outlets
adequate for the external peripherals, medical and test
equipment needed to support this Ultrasound system must also
be present within 1 m (3.2 ft.) of the Ultrasound system.
Electrical installation must meet all current local, state, and
national electrical codes.
If the Ultrasound system arrives without a power plug, or with
the wrong plug, you must contact your GE dealer or the
installation engineer must supply what is locally required.
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Power stability requirement
Table 2-4: Power stability requirement
IEC 61000-4-11
Voltage dips, short
interruptions and
voltage variations
on mains supply
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5
cycles;
70%T (30% dip) for 25
cycles;
< 5%T (>95% dip) for 5
sec
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5
cycles;
70%T (30% dip) for 25
cycles;
< 5%T (>95% dip) for 5
sec
Mains power
quality should be
that of a typical
commercial or
hospital
environment.
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EMI limitations
General Ultrasound system requirements
Ultrasound systems are susceptible to Electromagnetic
Interference (EMI) from radio frequencies, magnetic fields, and
transients in the air or wiring. They also generate EMI. The
Ultrasound system complies with limits as stated on the EMC
label. However there is no guarantee that interference will not
occur in a particular installation.
Possible EMI sources should be identified before the Ultrasound
system is installed.
Electrical and electronic equipment may produce EMI
unintentionally as the result of a defect. Some of these sources
include:
• medical lasers
• scanners
• cauterizing guns
• computers
• monitors
• fans
• gel warmers
• microwave ovens
• light dimmers
• mobile phones
• in-house wireless phones (DECT phones)
• wireless computer keyboard and mouse
• air conditioning system
• High Frequency (HF) surgery equipment
• general AC/DC adapters
The presence of a broadcast station or broadcast van may also
cause interference.
See: ‘EMI prevention/abatement’ on page 2-10 for EMI
prevention tips.
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EMI prevention/abatement
Table 2-5: EMI prevention/abatement
EMI RULEDETAILS
Be aware of Radio
Frequency sources
Ground the
Ultrasound system
Replace all screws,
Radio Frequency
gaskets, covers,
cores
Replace broken
Radio Frequency
gaskets
Do not place labels
where Radio
Frequency gaskets
touch metal
Use GE specified
harnesses and
peripherals
Take care with
cellular phones
Properly route
peripheral cables
• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI
sources.
• Special shielding may be required to eliminate interference problems caused by
high frequency, high powered radio or video broadcast signals.
Poor grounding is the most likely reason an Ultrasound system will have noisy
images. Check grounding of the power cord and power outlet.
• After you finish repairing or updating the Ultrasound system, replace all covers
and tighten all screws.
• Any cable with an external connection requires a magnet wrap at each end.
• Install all covers. Loose or missing covers or Radio Frequency gaskets allow
radio frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an Radio Frequency gasket are
broken, replace the gasket. Do not turn on the Ultrasound system until any loose
metallic part is removed.
Where applicable, never place a label where Radio Frequency gaskets meet the
Ultrasound system. Otherwise, the gap created will permit Radio Frequency
leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other
shielding. Also, cable length, material, and routing are all important; do not change
from what is specified.
Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
Where applicable, do not allow cables to lie across the top of the Card Rack or
hang out of the peripheral bays. Loop the excess length for peripheral cables
inside the peripheral bays. Attach the monitor cables to the frame.
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General Ultrasound system requirements
CAUTION
CAUTION
CAUTION
Probes environmental requirements
Operation, storage and transport temperatures for probes
Probes should be operated, stored, or transported within the
parameters outlined below.
Ensure that the probe face temperature does not exceed the
normal operation temperature range.
Table 2-6: Probe Environmental Requirements
OperationalStorageTransport
Temperature10° - 40° C
50° - 104° F
Humidity5 - 85%
non-condensing
Pressure700 - 1060hPa700 - 1060hPa700 - 1060hPa
0° - 55° C
32° - 131° F
5 - 85%
non-condensing
-40° - 55° C
-40° - 131° F
5 - 85%
non-condensing
Check the room temperature before you use the probe.
Ensure that the probe face temperature does not exceed the
normal operation temperature range.
NOTE: Refer to Table 2-1 on page 2-3 to determine the needed
settlement time.
Time and manpower requirements
Site preparation takes time. Begin site preparation checks as
soon as possible, if possible, six weeks before delivery, to allow
enough time to make any changes.
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Site Preparations
Contents in this section
• ‘Purchaser responsibilities’ on page 2-13
• ‘Required facility needs’ on page 2-14
• ‘Desirable features’ on page 2-15
• ‘Minimal floor plan suggestion’ on page 2-16
• ‘Recommended floor plan suggestion’ on page 2-17
• ‘Suggested floor plan, Ultrasound system, and EchoPAC PC
in same room’ on page 2-18
• ‘Networking setup requirements’ on page 2-18
Facility needs
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Purchaser responsibilities
The work and materials needed to prepare the site is the
responsibility of the purchaser. Delay, confusion, and waste of
manpower can be avoided by completing pre-installation work
before delivery. Purchaser responsibility includes:
• Procuring the materials required
• Completing the preparations before delivery of the
Ultrasound system
• Paying the costs for any alterations and modifications not
specifically provided in the sales contract
NOTE: All electrical installations that are preliminary to the positioning
of the equipment at the site prepared for the equipment must be
performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations, and testing
must also be performed by qualified personnel. The products
involved (and the accompanying electrical installations) are
highly sophisticated and special engineering competence is
required. All electrical work on these products must comply with
the requirements of applicable electrical codes. The purchaser
of GE equipment must only utilize qualified personnel to perform
electrical servicing on the equipment.
Facility needs
The desire to use a non–listed or customer provided product or
to place an approved product further from the Ultrasound
system than the interface kit allows, presents challenges to the
installation team. To avoid delays during installation, such
variances should be made known to the individuals or group
performing the installation at the earliest possible date
(preferably prior to the purchase).
The ultrasound suite must be clean prior to delivery of the
Ultrasound system. Carpet is not recommended because it
collects dust and creates static. Potential sources of EMI
(electromagnetic interference) should also be investigated
before delivery. Dirt, static, and EMI can negatively impact
Ultrasound system reliability.
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Site Preparations
Required facility needs
NOTE: GE requires a dedicated power and ground for the proper
operation of its Ultrasound equipment. This dedicated power
shall originate at the last distribution panel before the Ultrasound
system.
Sites with a mains power system with defined Neutral and Live
The dedicated line shall consist of one phase, a neutral (not
shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral
The dedicated line shall consist of one phase (two lines), not
shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
:
:
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Required facility needs (continued)
NOTE: Please note that image artifacts can occur, if at any time within
the facility, the ground from the main facility's incoming power
source to the Ultrasound unit is only a conduit.
• Dedicated single branch power outlet of adequate
amperage meeting all local and national codes which is
located less than 2.5 m (8 ft.) from the unit’s proposed
location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.5m (1.5 ft.) from the
wall for cooling
• Power outlet and place for any external peripheral are within
2 m (6.5 ft.) of each other with peripheral within 1 m of the
unit to connect cables.
• Power outlets for other medical equipment.
• Power outlets for test equipment within 1 m (3.2 ft.) of
Ultrsound system.
• Clean and protected space to store probes (in their cases or
on a rack)
• Material to safely clean probes (done with a plastic
container, never metal)
Facility needs
Desirable features
For the amperage requirements, see: ‘Electrical requirements’
on page 2-6.
• Door is at least 92 cm (3 ft.) wide
• Circuit breaker for dedicated power outlet is easily
accessible
• Sink with hot and cold water
• Receptacle for bio–hazardous waste, like used probe
sheaths
• Emergency oxygen supply
• Storage for linens and equipment
• Nearby waiting room, lavatory, and dressing room
• Dual level lighting (bright and dim)
• Lockable cabinet ordered by GE for its software and
proprietary manuals
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Site Preparations
4
1
3
11
6
13
8
10
5
7
9
12
14
2
Minimal floor plan suggestion
CSI 8x10
Scale:
Each square equals one square
foot (app. 31 x 31 cm)
1. Door – at least 762 mm (30
inches)
2. Film Viewer
3. Counter Top, Sink with hot
and cold water and Supplies
Storage
4. Linen Supply
5. Probes/Supplies
6. Examination Table – 1930 x
610 mm (76 x 24 inches)
7. Footswitch
8. Stool
9. Ultrasound system
10. External Peripherals
11. Dedicated Power Outlet Circuit Breaker protected and
easily accessible
12. Network Interface
13. 457 mm (18 inches) distance
of Ultrasound system from
wall or objects
14. GE Cabinet for Software and
Manuals
Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)
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Recommended floor plan suggestion
CSI 14x17
Facility needs
10
11
12
15
9
2
3
4
5
1314
16
8
7
1
17
6
18
Scale: Each square equals one square foot (app. 31 x 31 cm)
1. Secretaries or Doctors Desk
2. File Cabinet
3. Film Viewer
4. Counter Top
5. Counter Top and Sink with
hot and cold water
6. Overhead Lights Dimmer Dual Level Lighting (bright
and dim)
7. Emergency Oxygen
8. Suction Line
9. Ultrasound system
10. Dedicated Power Outlet Circuit Breaker protected and
easily accessible
11. Network Interface
12. 457 mm (18 inches) distance
of Ultrasound system from
wall or objects
13. Stool
14. Footswitch
15. Storage for Linens and
Equipment
16. Examination Table – 1930 x
610 mm (76 x 24 inches)
17. Lavatory and Dressing Room
18. Door – at least 762 mm (30
inches)
Figure 2-2. A 14 by 17 foot recommended floor plan
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Site Preparations
Suggested floor plan, Ultrasound system, and EchoPAC PC in same
room
1. EchoPAC PC workstation
parts
2. UPS
3. Ethernet network wall outlet
4. 3x mains power outlets
5. Hot and Cold water
6. Dedicated mains power outlet
7. Ethernet network wall outlet
Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner
Networking setup requirements
Stand alone Ultrasound system (without network connection)
None.
Scanner connected to hospital’s network
Supported networks:
10/100 Mbit Ethernet/DICOM network (option)
InSite requirements
InSite requires an Ethernet connection via:
• 10/100 Mbit Interface
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Purpose of the DICOM network function
DICOM services provide the operator with clinically useful
features for moving images and patient information over a
hospital network.
Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote
printers.
As an added benefit, transferring images in this manner frees up
the on-board monitor and peripherals, enabling viewing to be
done while scanning continues.
With DICOM, images can be archived, stored, and retrieved
faster, easier, and at a lower cost.
Facility needs
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Site Preparations
DICOM option setup requirements
To configure the Ultrasound system to work with other network
connections, the site’s network administrator must provide
information to complete the form “Worksheet for DICOM
Network Information”. Ensure that there are no spaces in any
field of the form.
See:
Entries must include:
• A host name, local port number, AE Title, IP address and
Net Mask for the Ultrasound system.
• The IP addresses for the default gateway and other routers
at the site for ROUTING INFORMATION.
• The host name, IP address, port and AE Title for each
device the site wants connected to the Ultrasound system
for DICOM APPLICATION INFORMATION. A field for the
make (manufacturer) and the revision of the device, is also
included. This information may be useful for error solving.
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DICOM option setup requirements (continued)
Facility needs
Figure 2-4. Worksheet for DICOM Network Information
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Site Preparations
Environmental Dangers
Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate AC
outlets, are in violation of patient safety standards. Suitable electrical isolation of such
external AC outlets, or providing the device with extra protective earth, will be required
in order to meet UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical
leakage.
Patient Vicinity UL60601-1 (USA)
2.12.20DV (UL60601-1:2003)
In area in which patients are normally cared for, the patient vicinity is the space with
surfaces likely to be contacted by the patient or attendant who can touch the patient.
This encloses a space within the room 1.83 m (6 ft.) beyond the perimeter of the bed
(examination table, dental chair, treatment booth, and the like) in its intended location,
and extending vertically 2.29 m (7.5 ft.) above the floor.
1. Patient environment
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Environmental Dangers
Patient Environment IEC60601-1 and ANSI AAMI ES60601-1
Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI
ES60601-1:2005)
Such an area is an environment in which medical diagnosis, monitoring or treatment is
carried out. It is very difficult to attach unique dimensions to the PATIENT
ENVIROMENT.
In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel
stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as
indicative of the dimensions of the Patient Environment.
The patient environment/vicinity will be depicted as a dashed line in this procedure.
See example below.
1. Patient environment
Figure 2-5.Patient environment
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Site Preparations
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Chapter 3
System Setup
This chapter contains information needed to install
LOGIQ C9 Series system.
Included is a procedure that describes how to receive
and unpack the equipment and how to file a damage or
loss claim.
How to prepare the facility and unit of the actual
installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are also
included in this procedure.
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System Setup
Contents in this chapter
• ‘Overview’ on page 3-2
• ‘Setup reminders’ on page 3-3
• ‘Receiving and unpacking the equipment’ on page 3-6
• ‘Preparing for setup’ on page 3-18
• ‘Completing the setup’ on page 3-19
• ‘System Configuration’ on page 3-22
• ‘Peripherals Installation Instructions’ on page 3-26
• ‘Connectivity setup’ on page 3-34
• ‘Paperwork after setup’ on page 3-40
Overview
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Average setup time
DANGER
CAUTION
CAUTION
CAUTION
Setup warnings
Setup reminders
Setup reminders
• Unpacking the LOGIQ C9 Series: 30 minutes
• Set up LOGIQ C9 Series wo/options: 30 minutes
• DICOM Network Configuration: 30 minutes or more,
depending on the configuration
• Install Insite: 0.5 hour
The LOGIQ C9 Series installation and functional checkout will
take approximately 1 hour. LOGIQ C9 Series consoles with
optional equipment may take slightly longer.
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE
OF OPENING THE AC GROUND LINE (I.E., METER’S
GROUND SWITCH IS OPEN), DON’T TOUCH THE
ULTRASOUND SYSTEM!
To prevent electrical shock, connect the unit to a properly
grounded power outlet. DO NOT use a three to two prong
adapter. This defeats safety grounding.
DO NOT wear the ESD wrist strap when you work on live
circuits and more than 30 V peak is present.
DO NOT operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.
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System Setup
DANGER
CAUTION
Setup warnings (continued)
1. There are no operator serviceable components. To prevent
shock, do not remove any covers or panels. Should
problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing.
NOTE: For information regarding packing labels, refer to LABELS
ON PACKAGE.
2. After being transported, the unit may be very cold or hot. If
this is the case, allow the unit to acclimate before you turn it
on. It requires one hour for each 2.5°C increment it's
temperature is below 10°C or above 40°C.
Equipment damage possibility. Turning the system on without
acclimation after arriving at site may cause the system to be
damaged.
If the Ultrasound system is very cold or hot, do not turn on its power
until it has had a chance to acclimate to its operating environment.
The following table describes guidelines for reaching operational
temperatures from storage or transport temperatures.
Table 3-1: System Acclimation Time Chart
Degree C50454035302520151050-5
Degree F122113104958677685950413223
hours4 2 0 000000246
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Setup warnings (continued)
CAUTION
CAUTION
Operator Manual(s)
The User Manual(s) should be fully read and understood
before operating the LOGIQ C9 Series and kept near the
Ultrasound system for quick reference.
Acoustic Output Hazard
Although the ultrasound energy transmitted from the LOGIQ
C9 Series probe is within AIUM/NEMA standards, avoid
unnecessary exposure. ultrasound energy can produce heat
and mechanical damage.
Setup reminders
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System Setup
CAUTION
CAUTION
Receiving and unpacking the
Purpose of this section
This section describes how to receive and unpack LOGIQ C9
Series.
Contents in this section
• ‘Warnings for receiving and unpacking’ on page 3-6
• ‘The Tilt indicator’ on page 3-7
• ‘Receiving the LOGIQ C9 Series’ on page 3-7
• ‘Unpacking the LOGIQ C9 Series’ on page 3-12
equipment
Warnings for receiving and unpacking
GENERIC CRT
VERSION
Two people are needed to unpack the Ultrasound system
because of its weight. Attempts to move the Ultrasound system
considerable distances or on an incline by one person could
result in injury or damage or both.
Two people are required whenever a part weighing 16 KG (35
LBS) or more must be lifted.
Remember to use relevant personal protecting equipment
(PPE) during packing and unpacking. Check with your local
EHS representative.
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Receiving and unpacking the equipment
The Tilt indicator
Overview
Improper handling during transportation may harm the
equipment inside the package even if the package itself is
undamaged.
To make it easier to detect if the handling during transportation
has been improper, a set of Tilt indicator has been attached to
the transportation box.
Table 3-2: Tilt Watch
DescriptionIllustration
Tilt Watch
Receiving the LOGIQ C9 Series
Overview
Improper handling during transportation may harm the
equipment inside the package even if the package itself is
undamaged.
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System Setup
Examine all packages
Examine package closely at time of delivery, as described in the
procedure below.
Table 3-3: Examine all packages
StepTaskIllustrations
1. Is damage apparent?
• If YES; continue with the instructions in
‘Damage in transportation’ on page 3-11.
• If NO; continue with the next step.
2. Is the Tilt Indicator red colored inside the
middle of the indicator?
• If YES: The Tilt Indicator has been
activated. Continue with the instructions in
‘Damage in transportation’ on page 3-11
before you continue with the next step.
• If NO: continue with the next step.
3. Continue with the instructions in ‘Unpacking
the LOGIQ C9 Series’ on page 3-12.
1 - Red Color
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Position of the Tilt indicator
The Tilt indicator has been attached to the transportation box as
illustrated in the figure below.
Receiving and unpacking the equipment
Figure 3-1. Tilt indicator
1. Tilt Indicator
NOTE: Before cutting the straps, check Tilt Tags to make sure it has not
been triggered. If damaged, report it to the carrier. If not, then
cut the straps around the crate.
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System Setup
If Tilt Indicator has triggered or is missing
The purpose of the tilt indicator label is to alert people handling a
product that it is sensitive to tipping and it must remain upright at
all times. It is basically an active "Up Arrow" that changes color if
the package is tipped89 degrees or more from horizontal.
These labels can be false activated if tipped less than 89
degrees, and shocked or vibrated at the same time. This event
does occur, but is considered uncommon. If a package is
received with an activated tilt indicator label, there is high
degree of certainty it tipped 89 degrees or more from horizontal
during shipment.
An activated tilt indicator label does not indicate if the package
was simply “Tipped” (laid down with no impact shock) or “Tipped
Over” (free fall, with an impact shock). Using both shock
indicator labels and tilt indicator labels will help identify if a Tip
Over impact shock occurred.
Table 3-4: Tilt Indicator has triggered or is missing
StepTask
1.
If the Tilt Indicator is missing:
Note on the shipping papers at the time of
receipt that the Tilt Indicator label is missing.
If the Tilt Indicator has triggered:
Note on the shipping papers at the time of
receipt that the Tilt Indicator label was activated.
2.
Inspect the product for possible concealed
damage.
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Receiving and unpacking the equipment
Damage in transportation
Follow this procedure if damage is apparent:
1. Write “Damage In Shipment” on ALL copies of the freight or
express bill BEFORE delivery is accepted or “signed for“ by
a GE representative or hospital receiving agent.
2. Report the damage to the carrier.
• Whether noted or concealed, damage MUST be
reported to the carrier immediately upon discovery, or in
any event, within 14 days after receipt, and the contents
and containers held for inspection by the carrier.
• A transportation company will not pay a claim for
damage if an inspection is not requested within this 14
day period.
LOGIQ C9 Series transportation box label
The LOGIQ C9 Series transportation box label is located at the
front of the transportation box.
Figure 3-2. LOGIQ C9 Series transportation box label 1
Figure 3-3. LOGIQ C9 Series transportation box label 2
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System Setup
CAUTION
Unpacking the LOGIQ C9 Series
When a new system arrives, check that any components are not
damaged and are not in short supply. If shipping damage or
shortage occurs, contact the address shown in Chapter 1.
Please carefully unpack the system, and do not dispose the
package of LOGIQ C9 Series, so that it can be reused for
service.
Table 3-5: Unpacking the LOGIQ C9 Series
StepDescriptionCorresponding Graphic
1Tear the stop open mark.
2Cut the two packing straps around the crate.
Note: To avoid injury, with one hand holding the
strap clasp when cutting the strap.
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Receiving and unpacking the equipment
Table 3-5: Unpacking the LOGIQ C9 Series
StepDescriptionCorresponding Graphic
3Remove the top cover.
4Open the four plastic locks.
Note: Rotate the inside plastic lock
counterclockwise to remove it and then remove
the outside lock.
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System Setup
Table 3-5: Unpacking the LOGIQ C9 Series
StepDescriptionCorresponding Graphic
5Remove the outside shipping box.
6Remove the dust bag from the unit and remove
the foam in the front of the control panel.
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Receiving and unpacking the equipment
Table 3-5: Unpacking the LOGIQ C9 Series
StepDescriptionCorresponding Graphic
7Remove the clear plastic (wrapped around the
LOGIQ C9 Series) from the unit.
Note: To avoid damaging the unit, please use a
pair of scissors instead of the knife.
8Remove the foams between the LCD and
control panel.
9Loosen the tie-down strap. Push the brass
piece to pull back handle, then loosen the strap.
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System Setup
Table 3-5: Unpacking the LOGIQ C9 Series
StepDescriptionCorresponding Graphic
10Remove the wooden ramp and attach it to the
Pallet base on the rear side of the
LOGIQ C9 Series.
11Pull the LOGIQ C9 Series down the Pallet base
ramp.
Note: Remember to pull the LOGIQ C9 Series
from the back for safer transportation.
12Remove all the covers and foams from the unit.
13Place all of the filling inside the Transportation
Box. Close the box, and store the filling for
possible future use.
Moving into Position
Please refer to User Manual on how to move the system.
Packing the Equipment
Please pack LOGIQ C9 Series in the reverse order of
unpacking.
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Packing materials - recycling information
Packing materials - recycling
information
The packing materials for LOGIQ C9 Series are recyclable:
• The Transportation Box is made of spruce or similar
material. (“PHYTOSANITARY CERTIFICATE” included in all
shipments to The People's Republic of China.)
• Lever lockings (hinges) are made of zinc plated steel.
• The inner reinforcements are made of Ethafoam
(Polyethylene foam).
• The plastic foil is made of LDPE (Low Density
Polyethylene).
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System Setup
Verify customer order
Compare items received by the customer to that which is listed
on the delivery order. Report any items that are missing, back
ordered, or damaged.
Physical inspection
Verify that the system arrived intact (visual inspection).
If the system has been damaged, please refer to ‘Damage in
transportation’ on page i-12 in the beginning of this manual.
Preparing for setup
EMI protection
The LOGIQ C9 Series has been designed to minimize the
effects of Electro-Magnetic Interference (EMI). Many of the
covers, shields, and screws are provided primarily to protect the
system from image artifacts caused by this interference. For this
reason, it is imperative that all covers and hardware are installed
and secured before the unit is put into operation.
See ‘EMI limitations’ on page 2-9 for more information about
EMI protection.
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Purpose of this section
This section describes how to complete the installation of
LOGIQ C9 Series.
Contents in this section
• ‘System specifications’ on page 3-19
• ‘Electrical specifications’ on page 3-20
• ‘Connections on the I/O Rear Panel’ on page 3-21
• ‘Connecting probes’ on page 3-21
• ‘Powering the system’ on page 3-21
Completing the setup
Completing the setup
System specifications
System requirements verification
• Verify that the site meets the requirements listed in
Chapter 2.
(See: ‘Facility needs’ on page 2-12.)
• Verify that the specifications below don’t conflict with any
on-site conditions.
Physical dimensions
Table 3-6: Physical dimensions of LOGIQ C9 Series
HeightWidthDepthDepth
1250700900
49.1227.5635.43
Console Weight
• Weight: approx. 130 kg (287 lbs)
mm
Inches
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System Setup
WARNING
Electrical specifications
Connecting a LOGIQ C9 Series to the wrong voltage level will
most likely destroy it.
Verification of the system’s voltage setting
Verify that the mains voltage specified for the LOGIQ C9 Series
is available on-site.
The voltage setting for the unit is found on a label near the
Mains Power Circuit Breaker on the rear of the system.
Refer to the latest revision User Manual for a fill list of product
labels.
Electrical specifications for LOGIQ C9 Series
In the table below, the electrical specifications for LOGIQ C9
Series includes monitor and on board peripherals.
Table 3-7: Electrical specifications for LOGIQ C9 Series
Part
Number
5489329LOGIQ C9 Premium for
5489330LOGIQ C9 Expert for
5489331LOGIQ C9 Expert for
5489332LOGIQ C9 Expert for
DescriptionVolta geTolerances
China
China (with 4D)
China
India
Power
consumntion
220-240V±10% Max.950VA50/60 Hz
220-240V±10% Max.950VA50/60 Hz
220-240V±10% Max.950VA50/60 Hz
220-240V±10% Max.950VA50/60 Hz
Frequency
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Connections on the I/O Rear Panel
NOTE: Accessory equipment connected to the analog and digital
interfaces must be certified according to the respective IEC
standards (e.g. IEC60950 for data processing equipment and
IEC60601-1 for medical equipment). Furthermore, all complete
configurations shall comply with the valid version of the system
standard IEC60601-1. Everybody who connects additional
equipment to the signal input part or signal output part of LOGIQ
C9 Series, configures a medical system, and is therefore
responsible that the Ultrasound system complies with the
requirements of the valid version of IEC60601-1. If in doubt,
consult the technical service department or your local
representative for GE Healthcare.
Connect Ethernet
Connect the network cable to the Ethernet connector on the I/O
Rear Panel.
The connector is located on the rear side of LOGIQ C9 Series.
Completing the setup
Connect USB Flash Drive
NOTE: USB Flash Drive approved for LOGIQ C9 Series are verified for
EMC performance according to EN55011 class B. The use of
any other USB Flash Drive will compromise this verification, and
may cause interference on LOGIQ C9 Series itself, or on other
electronic devices.
For approved models, please refer to Chapter 9.
Insert the USB Flash Drive in one of the USB ports on the
LOGIQ C9 Series.
Connecting probes
Please refer to User Manual on how to connect/disconnect a
probe.
Powering the system
Please refer to User Manual on how to power the system.
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System Setup
System Configuration
Purpose of this section
This section describes how to configure the LOGIQ C9 Series.
Contents in this section
LOGIQ C9 Series configuration
For complete instructions, refer to the lastest revision of the
LOGIQ C9 Series Basic User Manual, Chapter 16.
Information includes Entering Location, Adjusting Date and
Time, Selecting User interface Language, Selecting Online
Manual Language, Slelecting Unites of Measure.
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Overview
Peripherals Installation
Peripherals Installation
This section describes how to install and configure the
peripherals validated for the LOGIQ C9 Series.
For LOGIQ C9 Series peripheral list, please refer to ‘Peripheral’
on page 9-5 .
About the operation check-out of peripherals, See ‘Peripheral
checks’ on page 4-25 for more information.
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System Setup
Furnished materials
ItemDescriptionQuantityNote
1Sony UP-D897 MD Printer1
2Paper Roll1
3USB cable1
Table 3-9: Materials furnished with Color USB Printer
ItemDescriptionQuantityNote
This section describes the materials furnished with the
Peripherals and with the system.
Retain the original carton and packing materials in case
transport is needed in the future.
• B/W USB Printer
Table 3-8: Materials furnished with B/W Printer
• Color USB Printer
1Sony UP-D25MD Printer1
2Paper Roll1
3AC Power Cord (local purchase)1
4USB cable1
• Digital Printer
Table 3-10: Materials furnished with B/W Printer
ItemDescriptionQuantityNote
1HP Officejet 100 Printer1
2Paper Roll1
3USB cable1
• USB Stick
Table 3-11: Materials furnished with B/W Printer
ItemDescriptionQuantityNote
1SanDisk USB Stick1
2Paper Roll1
3USB cable1
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